C120006
Cyclopropyl methyl ketone
99%
Synonym(s):
Acetylcyclopropane
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About This Item
Linear Formula:
C3H5COCH3
CAS Number:
Molecular Weight:
84.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-146-4
Beilstein/REAXYS Number:
1633817
MDL number:
Assay:
99%
Form:
liquid
InChI key
HVCFCNAITDHQFX-UHFFFAOYSA-N
InChI
1S/C5H8O/c1-4(6)5-2-3-5/h5H,2-3H2,1H3
SMILES string
CC(=O)C1CC1
assay
99%
form
liquid
refractive index
n20/D 1.424 (lit.)
bp
114 °C (lit.)
density
0.849 g/mL at 25 °C (lit.)
Quality Level
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Related Categories
Application
- Synthesis of 1,2,4-trioxepanes and 1,2,4-trioxocanes via photooxygenation of homoallylic alcohols.: This study explores the synthesis of novel 1,2,4-trioxepanes and 1,2,4-trioxocanes through the photooxygenation of homoallylic alcohols, utilizing Cyclopropyl methyl ketone as a key reagent in the process. The findings highlight the efficiency and potential applications of this synthetic pathway in organic chemistry and pharmaceutical intermediate production (Singh et al., 2006).
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1C
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
69.8 °F - closed cup
flash_point_c
21 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Shigeo Hayashi et al.
Journal of enzyme inhibition and medicinal chemistry, 29(6), 846-867 (2014-02-13)
Because of the pivotal role of cyclooxygenase (COX) in the inflammatory processes, non-steroidal anti-inflammatory drugs (NSAIDs) that suppress COX activities have been used clinically for the treatment of inflammatory diseases/syndromes; however, traditional NSAIDs exhibit serious side-effects such as gastrointestinal damage
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